Changes in concentration profiles of polycyclic aromatic hydrocarbons (PAHs) from emission sources to various environmental media in the Pearl River Delta, China were investigated using fugacity modeling under steady state assumption. Both assumed evenly and observed unevenly distributed PAH moles emission profiles were applied. Applicability of the fugacity model was validated against the observed media PAH concentrations and profiles. At equal emission rates, the differences of media concentrations among various PAHs were as high as three (air) to seven (soil and sediment) orders of magnitude. Dramatic changes of PAH profiles from emission sources to various bulk environmental media also were demonstrated by using the actual emission rates. In general, the fractions of higher molecular weight PAHs in air and water were much lower than those at the emission sources, although the PAH profiles in soil and sediment were characterized by a significant reduction of lower molecular weight PAHs. It is likely that the field-measured median concentration profiles cannot be adopted directly for source apportionment without rectification. The most influential parameters affecting PAH profiles in the study area were emission rates, degradation rates, adsorption coefficient, Henry's law constant, PAH concentrations in upstream surface water, fugacity ratio, vapor pressure, and diffusion coefficient in air.